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21hydroxylasedeficiency 21ohd antiarrhythmics cardiology diagnosis differential endocrinology genetics hyponatremia pediatrics peds pharmacology phases
Classification, Differential Diagnosis, and Features of Hyponatremia According to Volume Status Hypervolemic hypernatremia - CHF
Classification, ... deficit - Salt-losing ... #Hyponatremia #Classification ... Differential #Diagnosis #Table ... #Causes
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... Severity depends ... #21HydroxylaseDeficiency #21OHD #pathophysiology
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
channels open leading ... Transient K+ efflux moving ... Vaughan Williams Classification ... #Pharmacology #Classification ... #Classes #pathophysiology
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